CLASS I Food recall · Reported 3 May 2017 · FDA Enforcement Report

Liquid Whey; Bulk recalled by Deutsch Kase Haus

Deutsch Kase Haus is recalling Liquid Whey; Bulk, distributed in 11 states. The recall was initiated on 5 Feb 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.
Quantity recalled2,220,253.9 lbs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1898-2017
FDA event ID
76426
Recalling firm
Deutsch Kase Haus, Middlebury, IN
Classification
Class I
Status
Terminated
Recall initiated
5 Feb 2017
FDA classified
24 Apr 2017
Reported
3 May 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Protein Powder

Timeline

5 Feb 2017Recall initiated by company
24 Apr 2017Classified by FDA+78 days
3 May 2017Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential Listeria monocytogenes contamination.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Liquid Whey; Bulk.

Where it was distributed

IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN

AlabamaArizonaIllinoisIndianaMichiganMinnesotaNevadaOhioPennsylvaniaTennesseeWisconsin

Questions about this recall

Is Liquid Whey; Bulk recalled?

Yes. Deutsch Kase Haus recalled Liquid Whey; Bulk on 5 Feb 2017. The recall is Class I and its status is Terminated. Recall number F-1898-2017.

Why was it recalled?

Potential Listeria monocytogenes contamination.

Which lots are affected?

All lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.

Where was it sold?

IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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